Low pathogenicity of anti-desmoglein 3 immunoglobulin G autoantibodies contributes to the atypical clinical phenotypes in pemphigus
Author:
Affiliation:
1. Department of Dermatology; Keio University School of Medicine; Tokyo Japan
2. Department of Dermatology; Cairo University School of Medicine; Cairo Egypt
3. Central Research Laboratory; Japan Blood Products Organization; Kobe Japan
Funder
the Ministry of Health, Labor and Welfare of Japan
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.12888/fullpdf
Reference9 articles.
1. Pemphigus, bullous impetigo, and the staphylococcal scalded-skin syndrome;Stanley;N Engl J Med,2006
2. Explanations for the clinical and microscopic localization of lesions in pemphigus foliaceus and vulgaris;Mahoney;J Clin Invest,1999
3. Pemphigus vulgaris with no mucosal lesions showing pemphigus-foliaceus-like skin manifestations: is there a ‘cutaneous type’ of pemphigus vulgaris?;Nagasaka;Dermatology,2005
4. Cutaneous pemphigus vulgaris with skin features similar to the classic mucocutaneous type: a case report and review of the literature;Shinkuma;Clin Exp Dermatol,2008
5. Cutaneous type pemphigus vulgaris: a rare clinical phenotype of pemphigus;Yoshida;J Am Acad Dermatol,2005
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